Masuda Michihito, Senda Joe, Watanabe Hirohisa, Epifanio Bagarinao, Tanaka Yasuhiro, Imai Kazunori, Riku Yuchi, Li Yuanzhe, Nakamura Ryoichi, Ito Mizuki, Ishigaki Shinsuke, Atsuta Naoki, Koike Haruki, Katsuno Masahisa, Hattori Nobutaka, Naganawa Shinji, Sobue Gen
a Department of Neurology and.
d Brain and Mind Research Center , Nagoya University , Nagoya.
Amyotroph Lateral Scler Frontotemporal Degener. 2016 Oct-Nov;17(7-8):571-579. doi: 10.1080/21678421.2016.1211151. Epub 2016 Aug 10.
We investigated common structural and network changes across the sporadic amyotrophic lateral sclerosis (ALS)-frontotemporal dementia (FTD) continuum. Based on cluster analysis using the frontotemporal assessment battery, 51 patients with sporadic ALS were subdivided into three groups: 25 patients with ALS with cognitive deficiency (ALS-CD); seven patients who satisfied FTD criteria (ALS-FTD), and 19 patients with ALS with normal cognitive function (ALS-NC). Compared with the controls, gray matter images from patients with ALS-FTD showed atrophic changes in the following order of severity: caudate head, medial frontal gyrus, thalamus, amygdala, putamen, and cingulate gyrus (peak level, uncorrected p < 0.001). The caudate head was significant at the cluster level using FWE correction (p < 0.05). Diffusion tensor imaging with tract-based spatial statistics revealed white matter changes in the areas surrounding the caudate head, the internal capsule, and the anterior horn of the lateral ventricle in the ALS-CD and ALS-FTD. Probabilistic diffusion tractography showed a significant decrease in structural connectivity between the caudate head and the dorsomedial frontal cortex and the lateral orbitofrontal cortex, even in the ALS-NC. Our results indicated that the caudate head and its networks were the most vulnerable to lesion in sporadic ALS-FTD-spectrum patients associated with cognitive decline with FTD features.
我们研究了散发性肌萎缩侧索硬化症(ALS)-额颞叶痴呆(FTD)连续体中的常见结构和网络变化。基于使用额颞叶评估量表的聚类分析,51例散发性ALS患者被分为三组:25例伴有认知缺陷的ALS患者(ALS-CD);7例符合FTD标准的患者(ALS-FTD),以及19例认知功能正常的ALS患者(ALS-NC)。与对照组相比,ALS-FTD患者的灰质图像萎缩变化严重程度依次为:尾状核头、额内侧回、丘脑、杏仁核、壳核和扣带回(峰值水平,未校正p<0.001)。使用FWE校正后,尾状核头在聚类水平上具有显著性(p<0.05)。基于纤维束的空间统计的扩散张量成像显示,ALS-CD和ALS-FTD患者尾状核头周围区域、内囊和侧脑室前角的白质发生变化。概率性扩散纤维束成像显示,即使在ALS-NC患者中,尾状核头与背内侧前额叶皮质和外侧眶额皮质之间的结构连接也显著减少。我们的结果表明,在伴有FTD特征的认知衰退的散发性ALS-FTD谱系患者中,尾状核头及其网络最易受损。